Canonical Allele Identifier: CA5800477
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs749734990
ExAC: 11:1093863 C / T
gnomAD v2: 11-1093863-C-T
gnomAD v3: 11-1099955-C-T
gnomAD v4: 11-1099955-C-T
MyVariant Identifiers: chr11:g.1093863C>T (hg19) chr11:g.1099955C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1099955C>T , CM000673.2:g.1099955C>T GRCh38
NC_000011.9:g.1093863C>T , CM000673.1:g.1093863C>T GRCh37
NC_000011.8:g.1083863C>T NCBI36
NG_051929.1:g.31982C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000361558.7:n.9739C>T
ENST00000674892.1:c.186C>T ENSP00000501871.1:p.Pro62=
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